Northern carmine bee-eaters can be found in a wide range of African savannah habitats, including deserts, woodlands, and occasionally the northern edges of the rainforest zone, although avoiding densely wooded areas. They also frequent agricultural fields of open pasture, flood-plains, and marshes, and have occasionally been seen searching for prey over large bodies of water. Their range is heavily centered around a band of loess deposits stretching across the width of the continent as they nest along rivers in these sandy cliffs. (Autin, 2019; Borrow and Demey, 2013; Fry, 2010; Fry and Fry, 2010; Fry, et al., 2020; McLaren, 2014)
Northern carmine bee-eaters are very brightly colored and easily distinguishable birds. Adults are a rosy carmine-pink with a bright, light blue rump and upper- and under-tail coverts. The head is an iridescent green-blue with a black eyeline, throat, and beak. They have long, dark red, pointed wings with remiges tipped in black. Underwings are buff in color. This species is sexually monomorphic, yet males are fractionally larger. Juveniles are not as bright in color overall, being a light, pale, dusky pink with pale red-brown wings and the same blue markings as adults. They are the largest of the bee-eaters, with an average length of 240-270 mm, excluding their long tail streamers which can reach up to 120 mm in length. The wingspan is an average of 147 mm. Weights range from 34-59 g. They can be distinguished from the southern carmine bee-eater, M. nubicoides, once considered a subspecies of , in that their chin is blue, whereas the Southern species has a carmine chin. (Autin, 2019; Borrow and Demey, 2013; Fry, 2010; McLaren, 2014)
Northern carmine bee-eaters are typically monogamous, although they have been documented mating outside their pairings, given the chance. They form pairs yearly, often with a previous partner, although not always. Nest parasitism has been documented in females and it is suspected that they also utilize helpers at the nest to aid in excavation or chick-rearing, much like other bee-eater species, although this has not been confirmed. (Elston, 2007)
Northern carmine bee-eaters are cavity nesters, which makes it difficult to observe reproductive behavior in the wild. Therefore, there are few accounts of their reproductive behaviors in a natural setting and most data has been gathered in a captive setting. Research has indicated that their geographic breeding range is highly correlated with a band of desert loess running across the 15°N latitude of Africa. Like many other bee-eaters, (Alba, 2019; Elston, 2007; Ferrie, 2016; Fry, 2010; McLaren, 2014)nest in tall vertical cliffs of loess and silt along large riverbanks, excavating tunnels, 1-2 meters long, where they will lay their eggs and raise young. They tend to prefer nests that are higher on the cliff face compared to lower ones. No substrate is used to line the nest, therefore broken eggshells are a common occurrence. 48% of hatchling deaths are due to starvation. breeds annually, with nest excavations beginning in April and laying beginning in May. Two to five eggs are laid, usually two days apart, and chicks hatch after around 20 days, and fledge after 23-30 days of rearing, usually in July.
Female northern carmine bee-eaters do much of the chick incubation both pre- and post-hatching, while the males guard the nest. However, the males later do most of the chick care and provisioning after incubation. Though, during all stages, both males and females aid in chick care. Brooding stops 13-19 days before fledging and will decrease in frequency until that point. During the last 8-11 days of the nestling stage, the parents will bring the chick live insects as food in order to initiate self-feeding. After fledging, the parents will continue to feed their young for up to two weeks. (Alba, 2019; Elston, 2007; Ferrie, 2016)
Not much information has been gathered about the lifespan of northern carmine bee-eaters, although it is believed that their average lifespan is around 7 years. However, the oldest known captive bird lived to be 17 years old at the San Diego Zoo. (Autin, 2019)
Territories are limited to claimed tunnels during breeding season. (Elston, 2007)
Northern carmine bee-eaters communicate with other members of their flock both visually and vocally. Visual displays include defensive posturing towards other birds, where the bird hunches downward with its head low and chest feathers puffed, and begging behavior performed by juveniles and breeding females for food items from males. Vocalizations vary and have different meanings, such as alarm, flight, greeting, courtship and more. Most commonly, throaty, loud, and punctuated flight calls are given en masse. (Autin, 2019; Borrow and Demey, 2013; Fry, 2010)
Northern carmine bee-eaters are insectivorous and prefer to feed upon locusts and grasshoppers, though they are opportunistic feeders. They catch and feed upon insects midair, and therefore are attracted to fires, which stir insects up into the air and make them available for capture. They have also been commonly seen using other animals, such as larger birds or ungulates, as perches, utilizing the movement of the other animal to stir up insects from the ground as well. Inedible insect parts are regurgitated as pellets. Food items are manipulated from the perch. For example, bee stingers are removed through rubbing the abdomen on the perch or other insects are paralyzed through beating. (Autin, 2019; Borrow and Demey, 2013; "Bulletin of the British Ornithologists’ Club, Volume 89", 1969; Fry, 2010; Fry and Fry, 2010; Mikula and Tryjanowski, 2016)
Not much information is known on the ecological impact of the northern carmine bee-eater, however, it is likely that, due to their large numbers, they are an important contributor to keeping insect populations in check. This is especially true for their preferred food source, locusts, as they have been recorded following locust movements across their range. (Autin, 2019; "Bulletin of the British Ornithologists’ Club, Volume 89", 1969; Fry and Fry, 2010; Mikula and Tryjanowski, 2016)has also been known to exhibit a commensal relationship with other species of animals including, but not limited to, bustards, ostriches, cattle, zebras, camels, antelope, and oryx, by using them as perches to more efficiently forage. This relationship also likely benefits these birds through predator protection and energy conservation as well. It is not known whether this relationship benefits the host species, as there is no evidence that feeds off of ectoparasites on the body of the host. It is also plausible that the breeding sites of provide microhabitats for other species that can benefit from new habitat and food sources provided through tunnel excavation.
The northern carmine bee-eater exhibits no great economic importance for humans. However, they are used both locally and nationally as a source of food, and their feathers can be used in adornments. Internationally, they are distributed in the pet trade or as zoological specimens, as they are attractive additions to any collection. However, since they are not easily bred in captivity, they are not common in this trade. There are less than 200 registered individuals in zoos globally. (Autin, 2019; Ferrie, 2016; "Northern Carmine Bee-eater", 2016)
There are no known adverse effects ofon humans.
While the northern carmine bee-eater is listed as Least Concern by the IUCN Red List, its populations are shown to be slightly decreasing. While the global population is currently unknown, they are common along rivers within their geographical range. There are currently no conservation or protective actions in place to preserve its populations. The cause of their decreasing population trend is likely due to factors such as over-hunting by humans for food, changing water levels due to the presence of hydro-electric dams, and riverbank collapse due to waves produced from speedboat traffic. ("Northern Carmine Bee-eater", 2016)
Skyler Mark (author), Northern Michigan University, Alec Lindsay (editor), Northern Michigan University, Tanya Dewey (editor), University of Michigan-Ann Arbor.
living in sub-Saharan Africa (south of 30 degrees north) and Madagascar.
uses sound to communicate
living in landscapes dominated by human agriculture.
young are born in a relatively underdeveloped state; they are unable to feed or care for themselves or locomote independently for a period of time after birth/hatching. In birds, naked and helpless after hatching.
having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.
an animal that mainly eats meat
uses smells or other chemicals to communicate
used loosely to describe any group of organisms living together or in close proximity to each other - for example nesting shorebirds that live in large colonies. More specifically refers to a group of organisms in which members act as specialized subunits (a continuous, modular society) - as in clonal organisms.
in deserts low (less than 30 cm per year) and unpredictable rainfall results in landscapes dominated by plants and animals adapted to aridity. Vegetation is typically sparse, though spectacular blooms may occur following rain. Deserts can be cold or warm and daily temperates typically fluctuate. In dune areas vegetation is also sparse and conditions are dry. This is because sand does not hold water well so little is available to plants. In dunes near seas and oceans this is compounded by the influence of salt in the air and soil. Salt limits the ability of plants to take up water through their roots.
animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.
parental care is carried out by females
A substance that provides both nutrients and energy to a living thing.
An animal that eats mainly insects or spiders.
offspring are produced in more than one group (litters, clutches, etc.) and across multiple seasons (or other periods hospitable to reproduction). Iteroparous animals must, by definition, survive over multiple seasons (or periodic condition changes).
parental care is carried out by males
marshes are wetland areas often dominated by grasses and reeds.
makes seasonal movements between breeding and wintering grounds
Having one mate at a time.
having the capacity to move from one place to another.
the area in which the animal is naturally found, the region in which it is endemic.
reproduction in which eggs are released by the female; development of offspring occurs outside the mother's body.
the business of buying and selling animals for people to keep in their homes as pets.
the kind of polygamy in which a female pairs with several males, each of which also pairs with several different females.
rainforests, both temperate and tropical, are dominated by trees often forming a closed canopy with little light reaching the ground. Epiphytes and climbing plants are also abundant. Precipitation is typically not limiting, but may be somewhat seasonal.
breeding is confined to a particular season
reproduction that includes combining the genetic contribution of two individuals, a male and a female
associates with others of its species; forms social groups.
uses touch to communicate
defends an area within the home range, occupied by a single animals or group of animals of the same species and held through overt defense, display, or advertisement
the region of the earth that surrounds the equator, from 23.5 degrees north to 23.5 degrees south.
A terrestrial biome. Savannas are grasslands with scattered individual trees that do not form a closed canopy. Extensive savannas are found in parts of subtropical and tropical Africa and South America, and in Australia.
A grassland with scattered trees or scattered clumps of trees, a type of community intermediate between grassland and forest. See also Tropical savanna and grassland biome.
A terrestrial biome found in temperate latitudes (>23.5° N or S latitude). Vegetation is made up mostly of grasses, the height and species diversity of which depend largely on the amount of moisture available. Fire and grazing are important in the long-term maintenance of grasslands.
uses sight to communicate
1969. Bulletin of the British Ornithologists’ Club, Volume 89. London: British Ornithologist's Club.
2016. "Northern Carmine Bee-eater" (On-line). The IUCN Red List of Threatened Species. Accessed January 30, 2020 at https://www.iucnredlist.org/species/22683768/92999759.
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Borrow, N., R. Demey. 2013. Field Guide to the Birds of Ghana. UK: Bloomsbury Publishing.
Burt, D. 2004. Plumage-Based Phylogenetic Analyses of the Merops Bee-Eaters. Ibis, vol. 146, no. 3: 481-492.
Elston, J. 2007. Use of Novel Nest Boxes by Carmine Bee-Eaters (Merops Nubicus) in Captivity. Zoo Biology, vol. 26, no. 1: 27-39. Accessed January 30, 2020 at doi:10.1002/zoo.20118.
Ferrie, G. 2016. Application of Video Recording Technology to Improve Husbandry and Reproduction in the Carmine Bee-Eater (Merops n. Nubicus). Zoo Biology, vol. 35, no. 1: 76-82.
Fry, H., P. Boesman, G. Kirwan. 2020. "Northern Carmine Bee-eater (Merops nubicus)" (On-line). Handbook of the Birds of the World Alive. Accessed January 30, 2020 at https://www.hbw.com/node/55852.
Fry, H. 2010. The Bee-Eaters. London: A & C Black.
Fry, H., K. Fry. 2010. Kingfishers, Bee-Eaters and Rollers. London: A & C Black.
McLaren, S. 2014. Loess and Bee-Eaters II: The ‘Loess’ of North Africa and the Nesting Behaviour of the Northern Carmine Bee-Eater (Merops Nubicus Gmelin 1788). Quaternary International, vol. 334–335: 112-118. Accessed January 30, 2020 at doi:10.1016/j.quaint.2014.01.040.
Mikula, P., P. Tryjanowski. 2016. Internet Searching of Bird-Bird Associations: A Case of Bee-Eaters Hitchhiking Large African Birds. Biodiversity Observations, vol. 80, no. 7: 1-6.